Flexible high-density mapping catheter

ABSTRACT

Aspects of the present disclosure are directed to flexible high-density mapping catheters with a planar array of high-density mapping electrodes near a distal tip portion. These mapping catheters may be used to detect electrophysiological characteristics of tissue in contact with the electrodes, and may be used to diagnose cardiac conditions, such as cardiac arrhythmias for example.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. provisional application No.62/414,634, filed 28 Oct. 2016, which is hereby incorporated byreference as though fully set forth herein.

BACKGROUND a. Field

The instant disclosure relates to high-density mapping catheters fordiagnosing, for example, cardiac arrhythmias, In particular, the instantdisclosure relates to flexible planar arrays including a plurality ofelectrodes positioned in a high-density array.

b. Background Art

Catheters have been used for cardiac medical procedures for many years.Catheters can be used, for example, to diagnose and treat cardiacarrhythmias, while positioned at a specific location within a body thatis otherwise inaccessible without a more invasive procedure.

Conventional mapping catheters may include, for example, a plurality ofadjacent ring electrodes encircling the longitudinal axis of thecatheter and constructed from platinum or some other metal. These ringelectrodes are relatively rigid. Similarly, conventional ablationcatheters may comprise a relatively rigid tip electrode for deliveringtherapy (e.g., delivering RF ablation energy) and may also include aplurality of adjacent ring, electrodes. It can be difficult to maintaingood electrical contact with cardiac tissue when using theseconventional catheters and their relatively rigid (or nonconforming),metallic electrodes, especially when sharp gradients and undulations arepresent.

When mapping a cardiac muscle, the beating of the heart, especially iferratic or irregular, makes it difficult to keep adequate contactbetween. electrodes and tissue for a sufficient length of time. Theseproblems are exacerbated on contoured, irregular, or trabeculatedsurfaces. If the contact between the electrodes and the tissue cannot besufficiently maintained, quality lesions or accurate mapping areunlikely to result.

The foregoing discussion is intended only to illustrate the presentfield and should not be taken as a disavowal of claim scope.

BRIEF SUMMARY

The instant disclosure relates to high-density mapping catheter tips fordiagnosing, for example, cardiac arrhythmias. In particular, the instantdisclosure relates to catheters with a planar array coupled to a distalend of a catheter shaft. The planar array includes a plurality ofelectrodes aligned in a high-density array to facilitate high-resolutionelectrophysiology mapping of tissue in contact with the plurality ofelectrodes.

Various embodiments of the present disclosure are directed to a planararray catheter including an elongated catheter shaft and a flexible,planar array. The elongated catheter shaft includes a proximal end and adistal end, and defines a catheter longitudinal axis extending betweenthe proximal and distal ends. The flexible, planar array is coupled tothe distal end of the catheter shaft, and includes two or more armsextending substantially parallel with the longitudinal axis and layingin a plane. Each of the arms conforms to tissue and includes a pluralityof electrodes mounted thereon. The plurality of electrodes are equallyspaced along both a length of each arm and across adjacent arms. In somespecific embodiments, the plurality of electrodes may sample electricalcharacteristics of contacted tissue in at least two substantiallytransverse directions.

Some aspects of the present disclosure are directed to anelectrophysiology mapping system including a planar array catheter andcontroller circuitry. The planar array catheter includes a cathetershaft, and a flexible, planar array coupled to a distal end of thecatheter shaft. The planar array conforms to tissue, and includes two ormore arms extending substantially parallel with the longitudinal axisand laying in a plane. Each of the arms have a plurality of electrodesmounted thereon with equal spacing along a length of each arm and acrossadjacent arms. The controller circuitry is communicatively coupled toeach of the plurality of electrodes, and samples electrical signalsreceived from each of the plurality of electrodes. In specificembodiments, the plurality of electrodes sample electricalcharacteristics of the contacted tissue, and the controller circuitryprocesses the sampled electrical. characteristics of the contactedtissue through an OIS/OT algorithm. The controller circuitry may producean output indicative of the true electrical characteristics of thecontacted tissue, independent of the orientation of the planar arraycatheter relative to the contacted tissue.

The foregoing and other aspects, features, details, utilities, andadvantages of the present disclosure will be apparent from reading thefollowing description and claims, and from reviewing the accompanyingdrawings.

BRIEF DESCRIPTION OF THE DRAWINGS

The patent or application file contains at least one drawing executed incolor. Copies of this patent or patent application publication withcolor drawings will be provided by the Office upon request and paymentof the necessary fee.

Various example embodiments may be more completely understood inconsideration of the following detailed description in connection. withthe accompanying drawings, in which:

FIG. 1A is a plan view of a planar array of an electrophysiologycatheter, consistent with various embodiments of the present disclosure.

FIG. 1B is an enlarged, fragmentary view of a proximal portion of theplanar array of FIG. 1A, consistent with various embodiments of thepresent disclosure.

FIG. 1C is an isometric view of the planar array portion shown in FIG.1B, consistent with various embodiments of the present disclosure.

FIG. 2 depicts the planar array catheter shown in FIGS. 1A-C with thearray of electrodes contacting tissue; consistent with variousembodiments of the present disclosure.

FIG. 3 depicts the planar array of the high-density mapping catheter ofFIGS. 1A-C overlaying vasculature, consistent with various embodimentsof the present disclosure.

FIG. 4A depicts an electrophysiology mapping interface, consistent withvarious embodiments of the present disclosure.

FIG. 4B depicts an electrophysiology mapping interface, consistent withvarious embodiments of the present disclosure.

FIG. 5 depicts an electrophysiology mapping interface, consistent withvarious embodiments of the present disclosure.

FIG. 6 depicts an electrophysiology mapping interface, consistent withvarious embodiments of the present disclosure.

FIG. 7 depicts a planar array in contact with an epicardial layer of acardiac muscle, consistent with various embodiments of the presentdisclosure.

FIG. 7A depicts the vertical, horizontal, and omnipole electrophysiologymaps based on the electrical data collected from the planar array ofFIG. 7 before ablation of the contacted tissue, consistent with variousembodiments of the present disclosure.

FIG. 7B depicts the vertical, horizontal, and omnipole electrophysiologymaps based on the electrical data collected from the planar array ofFIG. 7 after ablation of the contacted tissue, consistent with variousembodiments of the present disclosure.

While various embodiments discussed herein are amenable to modificationsand alternative forms, aspects thereof have been shown by way of examplein the drawings and will be described in detail. It should beunderstood, however, that the intention is not to limit the invention tothe particular embodiments described. On the contrary, the intention isto cover all modifications, equivalents, and alternatives falling withinthe scope of the disclosure including aspects defined in the claims. Inaddition, the term “example” as used throughout this application is onlyby way of illustration, and not limitation.

DETAILED DESCRIPTION OF EMBODIMENTS

Various embodiments of the present disclosure are directed to flexible,high-density mapping catheters. In general, the tip portions of thesehigh-density mapping catheters comprise an underlying support frameworkthat is adapted to conform to and remain in contact with tissue (e.g., abeating heart wall).

Aspects of the present disclosure are directed toward planar arraycatheters with substantially uniform spacing, and/or known and constantspacing, between electrodes which form bipole pairs forelectrophysiology mapping. More advanced embodiments of the presentdisclosure may utilize orientation independent sensing/omnipolartechnology (“OIS/OT”) and related algorithms to mitigate the need forsubstantially square electrode arrays. OIS/OT and related algorithms arediscussed in more detail in U.S. provisional application No. 61/944,426,filed 25 Feb. 2014, U.S. application Ser. No. 15/118,522, filed 25 Feb.2015, and international application no. PCT/US2014/011940, filed 16 Jan.2014, which are hereby incorporated by referenced as though fullydisclosed herein.

While some electrophysiology mapping catheters may consist of equallyspaced electrodes along a length of a planar array arm, the presentdisclosure is directed toward planar arrays with equal spacing ofelectrodes along both a length of the arms of the array, as well asbetween arms (i.e., x and y directions).

In some specific aspects of the present disclosure a planar arraycatheter including 7 arms is disclosed Each of the arms may be alignedwith, and extend parallel to, a longitudinal axis of the catheter shaft.Each arm is coupled to the other arms of the planar array at proximaland distal ends. The arms each include a row of electrodes extendingalong a length of the arm. The electrodes are evenly distributed alongthe length of the arm and between adjacent arms of the planar array.

Uniform spacing between adjacent electrodes in an array (in two or moredirections) facilitates simplified and robust OIS/OT-like assessments oforientation-specific electrical characteristics of myocardial tissue,for example. In some embodiments, orthogonal and identical spacingdirectly permits 2-directional assessments of electrical activationdirection and maximum voltage amplitude of sampled tissue. Moreover,uniform electrode spacing allows for the use of diagonal bipole pairswhich are orthogonal. (relative to one another), and substantiallymeasure the electrical characteristics of the same tissue area. Thevariation in readings between the orthogonal bipole pairs may beattributed to orientation-specific electrical characteristics of thecontacted tissue. Embodiments of the present disclosure may furtherfacilitate reduced complexity decimation by skipping intermediateelectrodes, and forming bipole pairs with larger electrode spacingconfigurations than created by adjacent electrodes in the array.Decimation may be used to determine electrical characteristics of tissueat a less granular resolution. Further, a clinician may assesssituational performance of the planar array at various bipole spacings.In various embodiments consistent with the present disclosure, adjacentbipole pairs may have various spacings, and be oriented in such a way asto facilitate various spatial orientations relative to one another.

The benefits of equal electrode spacing along two or more perpendiculardirections include an effective and simplified compensation scheme forsignals received from a clique (group) of electrodes, and six degrees offreedom (“DOF”) orientation and position information in. animpedance4yased navigation system's coordinate frame (e.g., the NavX™navigation. system manufactured by St. Jude Medical, Inc.). The six DOForientation and position information may be based on the determinedposition of the electrodes within the patient's body. A simplifiedcomputation of the electric field vector for cliques may be determinedbased only on average bipole voltages in the x, y (and possibly z)directions. Equal electrode spacing may also facilitate OIS/OT-likemethods that generate bipolar electrogram signals at variousorientations with respect to wavefronts so that a clinician may employarbitrary catheter orientations. Finally, the equal electrode spacing ofthe array facilitates a balanced and integrated view of voltage,fractionation, and:/or activation patterns, which may be readily sampledfrom adjacent electrodes with known/equal spacing. This information maythen be used to compute a divergence and curl (i.e., to detect/locatefoci and rotor cores from activation directions).

in some specific embodiments of an electrophysiology planar arraycatheter in accordance with the present disclosure, the planar array mayinclude 7 arms, each arm having 8 electrodes extending along a length ofthe arm with 2 millimeter (“mm”) spacing. The spacing between electrodesof adjacent arms also being 2 mm.

The electrodes disclosed herein may be ring electrodes, and/or printedelectrodes on substrates (e.g., flexible circuit boards).Advantageously, printed electrodes may be spaced more closely than ringelectrodes. In some embodiments, for example, printed electrodes spaced0.1 mm apart have been successfully deployed in a planar array catheter.More typically, ring electrodes and printed electrodes have beenadvantageously spaced 0.5 mm to 4 mm apart. It has. been found that suchelectrode spacing facilitates desirable electrophysiology mappinggranularity in a number of cardiovascular applications, for example.

Short interelectrode spacing (e.g., 2 mm×2 mm) may be desirable tosample electrical characteristics of tissue (e.g., voltages) indicativeof ablation line gaps. In testing, embodiments of the present disclosureincluding short interelectrode spacings of the electrode array detectedablation line gaps via the sampling of low voltage paths between lesionsonly separated by a few millimeters. Prior art electrophysiology mappingarrays, which lack the high-density electrode array and OIS/OTalgorithm-based electrogram signal processing of the present disclosure,are not capable of detecting such minute ablation line gaps.

Aspects of the present disclosure are directed toward planar arraycatheters and basket catheters for electrophysiology mapping. Morespecifically, many embodiments of the present disclosure utilize printedcircuit boards (e.g., flexible printed circuit boards) to form theplanar array arms and/or basket splines. Further, aspects of the presentdisclosure include a plurality of electrodes positioned along the planararray arms and/or basket splines. In such embodiments, the planar arrayarms and/or basket splines may have electrodes conductively coupled tothe flexible circuit board(s) that at least partially comprisestructures of the arms and/or splines. The resulting cliques (or groups)of independently addressable electrodes facilitate electrophysiologymeasurements of tissue, in contact with the electrodes, which areorientation independent. That is, measurements may be taken acrossbipole pairs of electrodes within each clique (with a known distancetherebetween) to capture measurements in at least two orientations. Inmore advanced 3D electrogram analysis, electrophysiology measurementsmay be captured in all three orientations. In some embodiments, it maybe desirable for the electrodes of a clique to be placed equidistant oneanother to facilitate enhanced electrogram fidelity. This equidistantpositioning of electrodes on a flexible circuit board may beaccomplished by existing. circuit board assembly techniques (e.g.,surface mount technology component placement systems, commonly referredto as “pick-and-place” machines and circuit board printing techniques).

Conventional mapping catheter designs employ bipole electrodeconfigurations to detect, measure, and display electrical signals fromthe heart. However, such conventional mapping catheter designs may beprone to error associated with the orientation of the bipole electrodepairs relative to an electrical wavefront of the heart, and result indisplayed signals and mapping results that may be orientation dependent,and may not actually reflect the true (or desired) tissue properties. Tomitigate this risk, aspects of the present disclosure are directed tosignal processing techniques which may sample a plurality of bipoleelectrode pair configurations, with varying orientations, to produceaccurate electrophysiology mapping results. To facilitate such signalprocessing techniques, electrophysiology mapping catheters consistentwith the present disclosure (e.g., linear, planar array, and basket) mayutilize cliques of electrodes that maintain spacing throughout varioustissue contact configurations.

Inventors of the present disclosure have discovered that certain bipoleelectrode pair arrangements, such as those aligned with an activationdirection of the electrical signals within the heart, show largeamplitude signals reflecting depolarization traveling through normal ornear normal tissue in contact with the bipole electrodes. Otheralignments of the bipole pairs, for example, where the bipole pairs arealigned perpendicular to an activation direction of the electricalsignals, or near scar tissue, may show lower amplitude fractionatedsignals. Various aspects of the present disclosure are directed toOIS/OT-like signal processing algorithms which separate signal amplitudeand signal directionality despite poorly controlled catheter-wavefrontorientation of the planar array.

For example, a first bipole pair of electrodes in an example cliquesamples an electrical signal passing through the contact tissue in anx-orientation, and a second bipole pair of electrodes in the cliquesamples a second electrical signal passing through the contact tissue ina y-orientation. Signal processing circuitry may then be used todetermine the true 2-dimensional. electrical signal for that location.The two bipole pairs, though substantially in the same location and incontact with the same tissue volume, may sample different electricalcharacteristics of the tissue due to the directionality of theelectrical activation wavefronts traveling through the heart. Forexample, the electrical activation wavefronts that typically emanatefrom a sinoatrial node, and atrioventricular node. However, interferingelectrical signals may also emanate from. one or more of the pulmonaryveins (e.g., arithmetic foci in the pulmonary vein(s)).

Importantly, to facilitate determination of important electricalcharacteristics of the tissue (e.g., impedance), the distance between afirst bipole pair and the distance between a second bipole pair must beknown and constant. In FIGS. 1A-C, the spacing of electrodes 102 _(1-N)on arms 103 ₁₋₇ are precise and constant. Furthermore, in variousembodiments it may be desirable for the distance between the two sets ofbipole pairs for a clique to be the same.

The use of high-density electrode arrays, disclosed herein, facilitatesthe sampling of voltage measurements, for example, that are independentof effects associated with relative orientation of the catheter andelectrical wavefront, making electrophysiology mapping of a cardiacmuscle (and scar borders) much more reliable and precise. Moreover,embodiments of the present disclosure benefit from the collection ofelectrical signal timing information which is substantially independentfrom the electrode distribution. The high-density array of electrodesmay also be used to verify sampled electrical signals from bipole pairs,by comparing the sampled electrical signal with other electrical signalssampled from adjacent (or nearby) bipole pairs. The regular spacing ofelectrodes in the high-density array further improves the accuracy ofvarious metrics which are output from the OIS/OT algorithms and/or othersignal processing techniques; for example, the En value (the estimate ofthe perpendicular bipole signal), an output of the Laplace equation,activation direction, conduction velocity, etc. Such aspects of thepresent disclosure are disclosed in more detail in U.S. provisionalapplication No. 61/944,426, filed 25 Feb. 2014, U.S. application Ser.No. 15/118,522, filed 25 Feb. 2015, and international application no.PCT/US2014/011940, filed 16 Jan. 2014, which are hereby incorporated byreferenced as though fully disclosed herein.

Details of the various embodiments of the present disclosure aredescribed below with specific reference to the figures.

FIG. 1A is a plan view of a planar array of an electrophysiology mappingcatheter 101 including a high-density array of electrodes 102 _(1-N),consistent with various embodiments of the present disclosure. Themapping catheter 101 includes a flexible tip portion 110 (also referredto as a planar array) that forms a flexible array of the electrodes 102_(1-N). This array of electrodes 102 _(1-N) is coupled to a flexibleframework of seven arms 103 ₁₋₇ which. extend in a plane that issubstantially parallel with a longitudinal axis of catheter shall 107.Each of the arms is precisely, laterally separated from each other tofacilitate exact spacing between electrodes 102 _(1-N) on adjacent arms103 ₁₋₇, and the arms are coupled to one another at a distal andproximal end of the flexible tip portion 110 (e.g., at a distal tip 109and bushing 106).

As shown in FIG. 1A, each of the seven arms 103 ₁₋₇ may carry aplurality of electrodes 102, with the spacing between each electrodebeing the same (or at least known). Similarly, the spacing betweenelectrodes 102 on adjacent arms 103 of the array may also be equal. Asshown by way of example, electrodes within a bipole pair 104 have acenter-to-center spacing of D_(A), and electrodes within a bipole pair104′, that is oriented substantially orthogonal relative to bipole pair104, have a center-to-center spacing of D_(B), where D_(A)-D_(B). Forexample, in some embodiments the center-to-center electrode spacing maybe between 0.5-4 mm. In yet more specific embodiments, thecenter-to-center electrode spacing may be less than 0.5 millimeters(e.g. 0.1 mm). While the present embodiment is directed to electrodepairs with equal center-to-center spacing, various other embodiments ofan electrode array consistent with the present disclosure may include anelectrode array with equal edge-to-edge spacing. For example, in someembodiments the edge-to-edge electrode spacing may be between 0.5-4 mamIn yet more specific embodiments, the edge-to-edge electrode spacing maybe less than 0.5 millimeters (e.g., 0.1 mm). Consideration ofedge-to-edge spacing may be desirable where the electrodes of the arrayhave different relative sizes (or surface areas).

Although the electrophysiology mapping catheter 101 in FIGS. 1A-Cdepicts seven arms, the catheters may comprise more or less arms, withspacing between each respective arm based on a desired electrode spacingfor a given electrophysiology application. Additionally, while theelectrophysiology mapping catheter 101 depicted in FIGS. 1A-C shows 56electrodes (e.g., 8 electrodes 102 on each arm 103), the catheters mayinclude, more or fewer than 56 electrodes, and each arm need not havethe same number of electrodes as adjacent arms.

In some embodiments, the electrodes 102 _(1-N). can be used indiagnostic, therapeutic, and/or mapping procedures. For example andwithout limitation, the electrodes 102 may be used forelectrophysiological studies, pacing, cardiac mapping, and ablation, insome embodiments, the electrodes 102 can perform unipolar or bipolarablation e.g., via the use of bipole pairs of electrodes 104 and 104′).This unipolar or bipolar ablation can create specific lines or patternsof lesions. In some embodiments, the electrodes 102 can. receiveelectrical signals from the heart, which can be used forelectrophysiological studies. Importantly, as the electrode spacingbetween adjacent electrodes on an arm 103, and those on. adjacent arms,are the same, bipole pairs 104 and 104′ with varying relativeorientations may be sampled to determine electrical characteristics ofthe tissue in contact with the bipole pairs. The sampled electricalcharacteristics may be processed to remove catheter orientation-basedsignal effects. In some embodiments, the electrodes 102 can perform alocation or position sensing function related to cardiac mapping;alternatively, ring electrodes 111 on a distal end of the catheter shaft107 may be used to determine location and/or orientation of the catheter101.

The flexible tip portion 110 of the catheter 101 is coupled to a distalend of a catheter shaft 107 at a bushing 106 (also referred to as aconnector). The catheter shaft 107 may also define a catheter shaftlongitudinal axis aa, as depicted in FIG. 1A. In the present embodiment,each of the arms 103 extend parallel to the longitudinal axis aa. Thecatheter shaft 107 may be made of a flexible material, such that it canbe threaded through a tortuous vasculature of a patient. In someembodiments, the catheter shaft 107 can include one or more ringelectrodes 111 disposed along a length of the catheter shaft 107. Thering electrodes 111 may be used for diagnostic, therapeutic,localization and/or mapping procedures, for example.

The planar array 110 may be adapted to conform to tissue (e.g., cardiactissue). For example, when. the planar array 110 contacts tissue, eacharm 103 ₁₋₇ may independently deflect to conform to the tissue. Theability for the planar array to deflect in response to tissue may beparticularly beneficial when the planar array comes into contact withcontoured, irregular, or trabeculated tissue. In some embodiments, thearms (or the understructure of the arms) may be constructed from aflexible or spring-like material such as nitinol and/or a flexiblesubstrate. The construction of the planar array arms 103 ₁₋₇ (including,for example, the length and/or diameter of the arms, and material) maybe adjusted or tailored to achieve desired resiliency, flexibility,foldability, conformability, and stiffness characteristics. Moreover, insome embodiments it may be desirable to vary one or more characteristicsfrom the proximal end of an arm to the distal end of the arm, or betweenor among the plurality of arms forming the planar array 110. Thefoldability of materials such as nitinol and/or a flexible substrateprovides the added benefit of facilitating insertion of the planar arrayinto a delivery sheath or introducer, whether dining delivery of thecatheter into the body or removal of the catheter from the body at theend of a procedure.

Planar array catheters including the high-density electrode arraypositioned thereon may be used for, for example: (1) defining regionalpropagation maps of particularly sized areas (e.g., one centimetersquare areas) on the walls of the heart; (2) identifying complexfractionated atrial electrograms for ablation; (3) identifyinglocalized, focal potentials between the microelectrodes for higherelectrogram resolution; and/or (4) more precisely targeting areas forablation. Electrophysiology mapping catheters, in accordance with thepresent disclosure, may be constructed to conform to, and remain incontact with, cardiac tissue despite potentially erratic cardiac motion.Such enhanced stability of the catheter on a heart wall during cardiacmotion provides more accurate mapping due to sustained tissue-electrodecontact. Additionally, the catheters described herein may findapplication in epicardial and/or endocardial use. For example, theplanar array embodiments depicted herein may be used in epicardialprocedures where the planar array of electrodes is positioned betweenthe myocardial surface and the pericardium. Alternatively the planararray embodiments may be used in endocardial procedure to sweep and/oranalyze the inner surfaces of the myocardium and create high-densitymaps of the heart tissue's electrical properties.

While various embodiments of the planar array 110 disclosed in thepresent disclosure are depicted with ring electrodes 102 _(1-N) coupledto the arms 103 ₁₋₇ (e.g., FIGS. 1A-C), embodiments with spot-typeelectrodes coupled to the arms are readily envisioned. Moreover, in yetfurther embodiments, the arms of the planar array may comprise flexiblethin films compatible with printed circuit manufacturing techniquesand/or have such thin films coupled to structural elements of the arm(e.g., nitinol-based arms). In such embodiments, spot-type electrodesmay be printed onto the arms themselves. In flexible printed circuitembodiments of the present disclosure, the printed electrodes may beelectrically coupled to signal processing. circuitry and/or drivercircuitry via traces extending on or within the one or more thin filmlayers. As many electrophysiology mapping applications require highsignal fidelity, it is desirable to limit the transmission length of theanalog signal, shield the transmission line itself, and/or convert theanalog signal to a digital signal close to the source of the analogsignal. Accordingly, aspects of the present disclosure are directed toplacing signal processing circuitry (e.g., analog-to-digital converters,signal conditioning such as noise filtration and bandpass filters),and/or driver circuitry on the arms 103 ₁₋₇ or in close proximitythereto.

In embodiments of the planar array including ring electrodes, the ringelectrodes of the high-density electrode array may include the same typeof electrode or a variety of various electrode types. For example,electrodes with smaller surface area may be used exclusively forelectrophysiology mapping, while larger surface area electrodes may beused for mapping, tissue ablation, and/or localization. In some specificembodiments, a most-distal ring electrode 102 on a first outboard arm103 ₁ may be slightly enlarged as is the most-proximal ring electrode ona second outboard arm 103 ₇. These slightly enlarged electrodes may beused, for example, for more precise localization of the flexible arrayin mapping and navigation systems. It may also be possible to driveablation current between these enlarged electrodes, if desired, forbipolar ablation, or, alternatively to drive ablation current inunipolar mode between one or both of these enlarged ring electrodes and,for example, a patch electrode located on a patient (e.g., on thepatient's back). Similarly, the electrodes 102 _(1-N) in someembodiments may all be capable of performing unipolar or bipolarablation therapies. Alternatively or concurrently, current could travelbetween one or more of the enlarged electrodes and any one or all of theelectrodes. This unipolar or bipolar ablation therapy technique may beused to create specific lesion lines or lesion patterns. As also seen inFIG. 1A, there may be a distal member (or ‘button’) 109 where one ormore of the arms 103 ₁₋₇ come together. This distal member 109 may beconstructed from metal or some other radiopaque material to providefluoroscopy visualization. The distal member 109 may further facilitate(semi-)independent planar movement between the arms 103 ₁₋₇.

FIG. 1B is an enlarged, fragmentary view of a proximal portion of theplanar array 110 of FIG. 1A, consistent with various embodiments of thepresent disclosure, in some embodiments of the present disclosure, theplanar array catheter may include one or more irrigant ports directedtoward the planar array. For example, in FIG. 1B, a distal tip 109 ofthe catheter shaft 107 may be fitted with one or more irrigant portsdirected toward the arms 103 ₁₄ of the array. The bushing 106 at thedistal end of the catheter shaft 107 couples each of the arms 103 to thecatheter shaft 107. In yet more specific embodiments, one or more of thearms 103 may include fluid lumens that extend to irrigant portspositioned along a length of one or more arms, and/or may extend to adistal tip 109 (as shown in FIG. 1A) where one or more irrigant portsare directed distally toward the planar array 110.

FIG. 1C is an isometric view of the planar array portion 110 shown inFIG. 1B with hidden lines showing a distal portion of the catheter shaft107. As shown in FIG. 1C, a sensor 116 (e.g., an impedance-basedlocation. sensor, a magnetic-based location sensor, etc) is mountedwithin/on the catheter shaft proximal to a bushing 106. A variety ofsensors may be implemented at this location, or at other locations, ofthe various high-density mapping catheters described herein. Thesesensors 116 may be mounted in the catheter shaft 107, as shown in FIG.1C, or may be mounted at other locations (e.g., along the electrodecarrying arms 103 ₁₋₇ of the high-density electrophysiology mappingcatheter and/or at the distal tip 109. In some specific embodiments, theplanar array may include two or more location sensors positioned on orabout the planar array to facilitate improved position and orientationidentification of the planar array within a patient. In one embodiment,the sensor 116 is a magnetic field sensor configured for use with anelectromagnetic localization system such as the MediGuide™ System soldby St. Jude Medical, Inc. of St. Paul, Minn.

FIG. 2 depicts a planar array catheter 200 including an array 210 ofelectrodes 202 ₁₋₈ contacting tissue 205. The tissue 205 in the presentembodiment is depicted as trabeculated, irregular, or contoured tissue.As shown in FIG. 2, the flexible arms of the planar array, includingflexible arm 203 ₁, conforms to the tissue 205, enabling a physician toplace the planar array 210 (and its electrodes 202 ₁₋₈) into constantcontact with the tissue 205. As a result, the electrical signals(indicative of the tissue's electrical activity) sampled by the planararray exhibit enhanced accuracy, and thereby have improved diagnosticvalue. Each of the flexible arms 203 ₁ include a plurality of electrodes202 ₁₋₈ which form cliques 204, and are coupled to the other adjacentarms of the planar array 210 at distal member 209 and bushing 206. Thebushing 206 further couples the planar array 210 to shaft 207.

FIG. 3 depicts a high-density mapping catheter 300 overlayingvasculature 301. In some embodiments of the present disclosure, thecatheter 300 may include steering wires which extend a length ofcatheter shaft 307. Prior to reaching a bushing 306 that couples thecatheter shaft 307 to arms 303 ₁₋₇ of planar array 310, the steeringwires may be coupled to steering rings which receive a tension from aproximal end of the steering wires and facilitates steering the cathetershall 307 and the planar array 310 through a patient's vasculature. Asfurther shown in FIG. 3, each of the arms 303 ₁₋₇ includes a pluralityof electrodes 302 _(1-N) distributed along a length of the arms. In thepresent embodiment, each of the electrodes are equally spaced from eachof its adjacent electrodes. When controller circuitry samples electricalsignals from bipole pairs of electrodes within the planar array 310,each of the bipole pairs will detect various electrical characteristicsindicative of the tissue health in. contact with the electrodes. Theseven arms 303 ₁₋₇ are designed to maintain the electrodes 302 _(1-N) ina spaced relationship so that each electrode captures electrophysiologydata of tissue at a known location relative to the other electrodes inthe array.

FIG. 4A depicts an electrophysiology mapping interface 401, consistentwith various embodiments of the present disclosure. Theelectrophysiology mapping interface 401 includes a plurality ofreal-time electrophysiology data streams 499 from various bipole pairsof electrodes across a planar array. A planar array visualizationportion 400 of the interface 401 presents a representation of the planararray 410. The representation of the planar array 410 may utilizelocalization data to orient and position the planar array within arendering of the cardiac muscle for example. Moreover, portions of theplanar array in contact with tissue may be visually indicated in theplanar array visualization 400. The green lines extending betweenelectrodes 402 _(1-N) on adjacent arms of the planar array 410 areindicative of a first configuration of bipole electrode pairs 440_(1-N). The electrical signals measured by the bipole pairs 440 _(1-N)presented in the real-time electrophysiology data streams 499. In thepresent embodiment, the electrical activation direction within thetissue in contact with the planar array 410 extends from a left-side ofthe visualization to the right-side. Accordingly, the bipole pairs 440_(1-N) are substantially aligned with the activation direction,resulting in electrogram data 499 from the bipole pairs 440 _(1-N) withrelatively high amplitudes. This data is indicative of the trueelectrical characteristics of the tissue in. contact with the planararray 410.

Upon receiving and processing electrogram data from the various bipolepairs of electrodes, the visualization 400 may be updated to color-code441 a surface of the cardiac muscle model displayed in the visualization(often referred to as an electrophysiology map). The electrophysiologymap may facilitate diagnosis by a clinician. For example, the clinicianmay use the mapped electrophysiology data to diagnose a cardiacarrhythmia (e.g., atrial fibrillation). To enable relative placement ofthe color-coded data 441 on the cardiac muscle model 442 in thevisualization, controller circuitry associates the electrogram data fromeach bipole pair 440 _(1-N) with a location the data was collected.Determination of the planar array's position within a cardiac muscle maybe facilitated by an impedance-based, electromagnetic, and/or hybridlocalization system.

FIG. 4B depicts an electrophysiology mapping interface 401′, consistentwith various embodiments of the present disclosure. Theelectrophysiology mapping interface 401′ includes a plurality ofreal-time electrophysiology data streams 499′ from various bipole pairsof electrodes 440′_(1-N) across a planar array 410. A planar arrayvisualization. 400′ portion of the interface 401′ presents arepresentation of the planar array 410. The representation of the planararray 41.0 may utilize localization data to orient and position theplanar array within a rendering of the cardiac muscle 442′, for example.Moreover, portions of the planar array 410 in contact with tissue may bevisually indicated in the planar array visualization 400′. The red linesextending between electrodes 402 _(1-N) on adjacent arms of the planararray 410 are indicative of a second configuration of bipole electrodepairs 440′_(1-N). The electrical signals measured by the secondconfiguration of bipole pairs are presented in the real-timeelectrophysiology data streams 499′. The data streams for each of thebipole pairs are collected simultaneously. In the present embodiment,the electrical activation direction within the tissue in contact withthe planar array 410 extends from a left-side of the visualization tothe right-side. Accordingly, the bipole pairs 440′_(1-N) extendsubstantially orthogonal to the activation direction, resulting inelectrogram data from the bipole pairs 440′_(1-N) with relatively lowamplitudes. This data is not indicative of the true electricalcharacteristics (e.g., maximal bipole amplitude characteristics) of thetissue in contact with the bipole pairs.

FIG. 5 depicts an electrophysiology mapping interface 501, consistentwith various embodiments of the present disclosure. Theelectrophysiology mapping interface 501 includes a plurality ofreal-time electrophysiology data streams 599 from various bipole pairsof electrodes across a planar array 510. A planar array visualizationportion 500 of the interface 501 presents a representation of the planararray. As shown in FIG. 5, the representation of the planar arrayutilizes localization data to orient and position the planar arraywithin a rendering of a cardiac muscle 542. The arrows are illustrativeof an activation direction 543 of the electrical signals travellingthrough the cardiac muscle. The green lines extending between electrodes502 _(1-N) on adjacent arms attic planar array 510 are illustrative of afirst configuration of bipole electrode pairs 540 _(1-N). The electricalsignals measured by the first configuration of bipole pairs 540 _(1-N)are presented as the green electrophysiology data streams 556. The redlines extending between electrodes 502 _(1-N) on adjacent arms of theplanar array are illustrative of a second configuration of bipoleelectrode pairs 540′_(1-N). The electrical signals measured by thesecond configuration of bipole pairs 540′_(1-N) are presented as the redelectrophysiology data streams 555.

The electrophysiology data streams 556 of the first bipole pairs 540_(1-N) show an increase in signal amplitude from the top left of theplanar array 510 to the bottom right. The larger amplitude signals areindicative of depolarization traveling through. normal or near normalmyocardial tissue in contact with the bipole electrodes. Accordingly,the top-left of the planar array is color-coded 541 red to indicate lesshealthy tissue, with the more healthy tissue to the right and bottom ofthe screen being coded with. greens and blues to indicate mare healthytissue. The red coded tissue may be (near) scar tissue, for example, andmay be a point of interest for

The red electrophysiology data streams 555 show (fractionated)electrograms with low amplitude thresholds across the planar array 510.This is because the bipole pairs in the second configuration 540′_(1-N)are aligned perpendicular to the activation direction 543 of theelectrical signals. Due to the undesirable orientation, substantiallyorthogonal, between the second configuration of bipole pairs 540′_(1-N)and the activation direction 543 of electrical signals through thecardiac muscle, the red electrophysiology data streams 555 do notrepresent the greatest possible local bipole voltage and thus maymisrepresent a scar.

FIG. 6 depicts an electrophysiology mapping interface 601, consistentwith various embodiments of the present disclosure. Signal processingcircuitry may utilize OIS/OT features, such as wave crest direction, todetermine which fractionated electrograms 602 to ignore when developingan electrophysiology map 600 of a cardiac muscle. As a result, aclinician need not re-orient a planar array 610 on target tissue toverify that an electrogram signal is representative of the trueactivation signal traveling through the target tissue. Signal processingcircuitry may further determine an activation. direction 643 when thefirst and second configuration of bipole electrode pairs are bothorientated approximately 45′ from an activation direction 643. In such acase, the electrogram signals 602 from the first and second bipoleelectrode pairs (640 ₁₋₂ and 640′₁₋₂, respectively) of a target tissuewill exhibit substantially the same signal. Both sets of signals exhibitsimilar local activity resolution and far field components.

FIG. 7 depicts a planar array 701 in contact with an epicardial layer ofa cardiac muscle 700, consistent with various embodiments of the presentdisclosure.

FIG. 7 shows the cardiac muscle 700 after tissue ablation therapy hasbeen conducted. The resulting ablation lesions 702 _(A-B) appear on thesurface of the cardiac muscle 700 as white spots. To conduct anelectrophysiology mapping of the cardiac muscle in proximity to theablation locations, both before and after the ablation therapy, pacingis conducted from epicenter 799. Adjacent electrodes 703 _(1-N) areassigned to bipole pairings. During the pacing procedure, each bipolepair samples the electrical characteristics of the tissue in between thepair. The resulting electrical signals are received and processed bycontroller circuitry. The controller circuitry develops anelectrophysiology mapping by associating the signal samples from eachbipole pair with a location of the tissue sampled by the bipole pair.The electrogram from each bipole pair may be analyzed and variouselectrical characteristics may be visually indicated on anelectrophysiology map by color-coding (or other visual indicationscheme, e.g., shading, patterning, etc.). In some embodiments, thecolor-coding may be based on the electrogram voltage at each location(e.g., mean, average, max, etc.). In other embodiments, the number oftimes the electrical signal exceeds a threshold voltage (or a voltageslope changes signs) during a sampling window may be visually displayedon the map. In yet other embodiments, total energy sampled during a timewindow may be displayed. Various other methods of fractionationaccounting are known and may be used as one or more factors of theresulting color-code displayed on the electrophysiology map.

FIG. 7A depicts the vertical, horizontal, and omnipole electrophysiologymaps based on the electrical data collected from the planar array 710 ofFIG. 7 before ablation of the contacted tissue. The vertical 705,horizontal 710, and omnipole 715 electrophysiology maps indicate thatthe tissue in contact with the planar array 710 is generally healthy.However, both the vertical 705 and horizontal 710 bipole maps evidencefalse-positive regions 704 _(A-B) due to misaligned orientations of theactivation direction of the electrical signals flowing through thecardiac muscle 700, and the bipole pairs' orientation. Specifically, asshown in FIG. 7, the activation direction emanates from epicenter 799,and moves down and to the left through the electrophysiology map shownin FIGS. 7A-B. As a result, both the vertical and horizontalelectrophysiology maps 705 and 710 visually indicate moderatelyunhealthy tissue at the false-positive regions 704 _(A-B). A positivetissue identification region may be defined by a low voltage signal thatis actually indicative of completely ablated tissue. The omnipoleelectrophysiology map 715 is devoid of orientation-relatedfalse-positive regions, due to the controller circuitry sampling bipolepairs in each tissue region with substantially orthogonal orientationrelative to one another. The controller circuitry may include signalprocessing circuitry which utilizes OIS/OT type algorithms to filter outlow amplitude signals from bipole pairs that are misaligned with theactivation direction of the pacing signal. Alternatively, thefunctionality of the OIS/OT type algorithms may be partially orcompletely conducted by a clinician manually. For example, a clinicianmay analyze an electrophysiology map using horizontal bipole pairs,followed by an analysis of a second electrophysiology map using verticalbipole pairs.

FIG. 7B depicts the vertical 705′, horizontal 710′, and omnipole 715′electrophysiology maps based on the electrical data collected from theplanar array of FIG. 7, after ablation of the contacted tissue. Whileall three electrophysiology mapping methodologies identify the newlyformed scar tissue at the ablation sites 702 _(A-B) (due to the changein electrical activity caused by the necrosis of the tissue), thevertical 705′ and horizontal 710′ electrophysiology maps also detectfalse-positive regions 704 _(C-D).

The false-positive region 704 _(C) in the vertical map 705′ is lesssevere than the false-positive region 704 _(D) in the horizontal map710′ as the pacing source is positioned at the top-right of the map (seeepicenter 799 in FIG. 7). Accordingly, activation direction of thepacing is substantially in-line with the vertical bipole pairarrangements in the vertical map 705′, and orientated largely orthogonalto the horizontal bipole pairs sampled in the horizontal map 710′. Asthe omnipole map 715′ looks at both vertical and horizontal bipolearrangements, these false-positive regions are largely eliminatedproviding a clinician with an electrophysiology map which moreaccurately depicts the true health of the tissue. For example, in anatrial fibrillation therapy, the clinician after analyzing the omnipoleelectrophysiology map 715′ may determine that an additional spotablation may be necessary between ablation sites 702 _(A-B) to fullyblock the flow of stray electrical signals from one or more of thepulmonary veins in the left atrium.

As shown in FIG. 7B, the clinician, when looking at horizontalelectrophysiology map 710′ in isolation, may falsely establish theefficacy of the ablation therapy. The likelihood of such an event may begreatly increased where the activation direction is not otherwise knownby the clinician (as opposed to a known pacing electrode position). Insuch a case, the clinician would need to rotate the planar array aboutthe longitudinal axis in order to detect the false reading. However,such repositioning of the planar array may be limited by physicalconstraints within, for example, the left atrium of a cardiac muscle.

While various embodiments of high-density electrode catheters aredisclosed herein, the teachings of the present disclosure may be readilyapplied to various other catheter embodiments as disclosed, for example,in the following patents and patent applications which are herebyincorporated by reference: U.S. provisional application No. 61/753,429,tiled 16 Jan. 2013; U.S. provisional application No. 60/939,799, filed23 May 2007; U.S. application Ser. No. 11/853,759 filed 11 Sep. 2007,now U.S. Pat. No. 8,187,267, issued 29 May 2012; U.S. provisionalapplication No. 60/947,791, filed 3 Jul. 2007; U.S. application Ser. No.12/167,736, filed 3 Jul. 2008, now U.S. Pat. No. 8,206,404, issued 26Jun. 2012; U.S. application Ser. No. 12/667,338, filed 20 Jan. 2011 (371date), published as U.S. patent application publication no. US2011/0118582 A1; U.S. application Ser. No. 12/651,074, filed 31 Dec.2009, published as U.S. patent application publication no. US2010/0152731 A1; U.S. application Ser. No. 12/436,977, filed 7 May 2009,published as U.S. patent application publication no. US 2010/0286684 A1;U.S. application Ser. No. 12/723,110, filed 12 Mar. 2010 published asU.S. patent application publication no. US 2010/0174177; U.S.provisional application No. 61/355,242, filed 16 Jun. 2010; U.S.application Ser. No. 12/982,715, filed 30 Dec. 2010, published as U.S.patent application publication no. US 2011/0288392 A1: U.S. applicationSer. No. 13/159,446, filed 14 Jun. 2011, published as U.S. patentapplication publication no. US 2011/0313417 A1; internationalapplication no. PCT/US2011/040629, filed 16 Jun. 2011, published asinternational publication no. WO 2011/159861 A2; U.S. application Ser.No. 13/162,392, filed 16 Jun. 2011 published as U.S. patent applicationpublication no. US 2012/0010490 A1; U.S. application Ser. No.13/704,619, filed 16 Dec. 2012, which is a national phase ofinternational patent application no. PCT/US2011040781, filed 16 Jun.2011, published as international publication no. WO 2011/159955 A1.

While various embodiments of the present disclosure are directed to theuse of high-density electrode catheters in conjunction with OIS/OTalgorithms, the teachings of the present disclosure may be readilyapplied to various other algorithm types. For example, embodimentsconsistent with the present disclosure may utilize the electrode signalpost-processing techniques, and electrophysiology mapping algorithmsdisclosed in the following publications, which are hereby incorporatedby reference: Magtibay et al. JAHA 2017 (J Am Heart Assoc. 2017;6:e006447, DOI: 10.1161/JAHA.117.006447) (see, e.g., pages 6 and 7, andsection titled “Omnipoles Provide the Largest Possible BipolarVoltages”); and Haldar et al. Circulation AE 2017 (Circ ArrhythmElectrophysiol. 2017; 10:e005018.DOI: 10.1161/CIRCEP.117.005018) (see,e.g., page 6, section titled “Omnipolar Voltage Amplitude Correlates toLargest Measurable Bipolar Vpp,” and FIG. 4).

Although several embodiments have been described above with a certaindegree of particularity, those skilled in the art could make numerousalterations to the disclosed embodiments without departing from thespirit of the present disclosure. It is intended that all mattercontained in the above description or shown in the accompanying drawingsshall be interpreted as illustrative only and not limiting. Changes indetail or structure may be made without departing from the presentteachings. The foregoing description and following claims are intendedto cover all such modifications and variations.

Various embodiments are described herein of various apparatuses,systems, and methods. Numerous specific details are set forth to providea thorough understanding of the overall structure, function,manufacture, and use of the embodiments as described in thespecification and illustrated in the accompanying drawings. It will beunderstood by those skilled in the art, however, that the embodimentsmay be practiced without such specific details. In other instances,well-known operations, components, and elements have not been describedin detail so as not to obscure the embodiments described in thespecification. Those of ordinary skill in the art will understand thatthe embodiments described and illustrated herein are non-limitingexamples, and thus it can be appreciated that the specific structuraland functional. details disclosed herein may be representative and donot necessarily limit the scope of the embodiments, the scope of whichis defined solely by the appended claims.

Reference throughout the specification to “various embodiments,” “someembodiments,” “one embodiment,” “an embodiment,” or the like, means thata particular feature, structure, or characteristic described inconnection with the embodiment is included in at least one embodiment.Thus, appearances of the phrases “in various embodiments,” “in someembodiments,” “in one embodiment,” “in an embodiment,” or the like, inplaces throughout the specification are not necessarily all referring tothe same embodiment. Furthermore, the particular features, structures,or characteristics may be combined in any suitable manner in one or moreembodiments. Thus, the particular features, structures, orcharacteristics illustrated or described in connection with oneembodiment may be combined, in whole or in part, with the featuresstructures, or characteristics of one or more other embodiments withoutlimitation.

It will be appreciated that the terms “proximal” and “distal” may beused throughout the specification with reference to a clinicianmanipulating one end of an instrument used to treat a patient. The term“proximal” refers to the portion of the instrument closest to theclinician and the term “distal” refers to the portion located furthestfrom the clinician. It will be further appreciated that for concisenessand clarity, spatial terms such as “vertical,” “horizontal,” “up,” and“down” may be used herein with respect to the illustrated embodiments.However, surgical instruments may be used in. many orientations andpositions, and these terms are not intended to be limiting and absolute.

Any patent, publication., or other disclosure material, in whole or inpart, that is said to be incorporated by reference herein isincorporated herein only to the extent that the incorporated materialsdoes not conflict with existing definitions, statements, or otherdisclosure material set forth in this disclosure. As such, and to theextent necessary, the disclosure as explicitly set forth hereinsupersedes any conflicting material incorporated herein by reference.Any material, or portion thereof, that is said to be incorporated byreference herein, but which conflicts with existing definitions,statements, or other disclosure material set forth herein will only beincorporated to the extent that no conflict arises between thatincorporated material and the existing disclosure material.

1-20. (canceled)
 21. A planar array catheter comprising: an elongatedcatheter shaft defining a catheter longitudinal axis extending between aproximal end and a distal end; and a flexible, planar array at thedistal end of the catheter shaft, the planar array configured to conformto tissue, and including two or more arms extending substantiallyparallel with the longitudinal axis and lying in a common plane, each ofthe arms having a plurality of electrodes mounted thereon; wherein theplurality of electrodes are configured to: detect anelectrophysiological characteristic of tissue in contact with the planararray; output signals indicative of the detected electrophysiologicalcharacteristic of the tissue; and selectively ablate the tissue based atleast in part on the detected electrophysiological characteristic of thetissue.
 22. The planar array catheter of claim 21, wherein the pluralityof electrodes are equally spaced along both a length of each arm andacross adjacent arms.
 23. The planar array catheter of claim 21, whereinthe plurality of electrodes are further configured to selectively ablatethe tissue using unipolar ablation.
 24. The planar array catheter ofclaim 21, wherein the plurality of electrodes are further configured toselectively ablate the tissue using bipolar ablation.
 25. The planararray catheter of claim 21, wherein three or more electrodes of theplurality of electrodes form a clique, the clique configured to sampleelectrical characteristics of a particular point of the contacted tissuein at least two substantially transverse directions, and the sampledelectrical characteristics in at least one of the at least twosubstantially transverse directions are independent of the orientationof the planar array catheter relative to the tissue and therebyindicative of the true electrical characteristics of the particularpoint of the contacted tissue.
 26. The planar array catheter of claim25, wherein the clique of the plurality of electrodes includes two ormore bipole electrode pairs that extend diagonally across adjacent armsof the planar array.
 27. The planar array catheter of claim 25, whereinthe clique of the plurality of electrodes includes two or more bipoleelectrode pairs that extend along an arm of the planar array and acrossthe arm and an adjacent arm of the planar array.
 28. The planar arraycatheter of claim 21, wherein the plurality of electrodes include: afirst plurality of electrodes configured to detect theelectrophysiological characteristics of the tissue; and a secondplurality of electrodes with a larger surface area compared to the firstplurality of electrodes, the second plurality of electrodes configuredto perform at least one of the following: detect theelectrophysiological characteristics of the tissue, conduct selectivetissue ablation, and conduct localization.
 29. The planar array catheterof claim 21, wherein the center-to-center distance between adjacentelectrodes of the plurality of electrodes is between 0.1 and 4millimeters.
 30. An electrophysiology system comprising: a planar arraycatheter including; a catheter shaft; a flexible, planar array coupledto a distal end of the catheter shaft, the planar array configured toconform to tissue, and including two or more arms extendingsubstantially parallel with the longitudinal axis and lying in a commonplane, each of the arms having a plurality of electrodes mountedthereon, the plurality of electrodes equally spaced along a length ofeach arm and across adjacent arms and configured to sample electricalcharacteristics of the contacted tissue; and controller circuitrycommunicatively coupled to each of the plurality of electrodes andconfigured to: sample electrical signals from each of the plurality ofelectrodes indicative of the electrical characteristics of the tissue inclose proximity to each of the respective electrodes; process thesampled electrical signals to determine electrophysiologicalcharacteristics of the tissue; and selectively ablate the tissue basedat least in part on the detected electrophysiological characteristics ofthe tissue.
 31. The electrophysiology system of claim 30, wherein thecontroller circuitry is further configured to process the sampledelectrical signals by determining the true electrical characteristics ofthe contacted tissue independent of the orientation of the planar arraycatheter relative to the contacted tissue.
 32. The electrophysiologysystem of claim 30, wherein the controller circuitry is furtherconfigured to: identify a clique of adjacent electrodes of the pluralityof electrode including first and second bipole electrode pairs thatextend substantially orthogonal relative to one another across thetarget tissue; and sample electrical characteristics of the tissueacross the first and second bipole electrode pairs; wherein theprocessing of the sampled electrical signals further includesassociating the sampled electrical characteristics of the tissue acrossone of the first and second bipole electrode pairs with the trueelectrical characteristics of the particular point of the contactedtissue.
 33. The electrophysiology system of claim 32 wherein thecontroller circuitry is further configured to process the sampledelectrical characteristics from the first and the second set of bipoleelectrodes through an OIS/OT algorithm, and to determine the trueelectrical characteristics of the contacted tissue independent of theorientation of the first and second set of bipole electrodes relative tothe contacted tissue.
 34. The electrophysiology system of claim 30,wherein the planar array includes bipole electrode pairs that extenddiagonally across adjacent arms of the planar array.
 35. Theelectrophysiology system of claim 30, wherein the center-to-centerdistance between adjacent electrodes of the plurality of electrodes isbetween 0.1 and 4 millimeters
 36. The electrophysiology system of claim30, further including a display communicatively coupled to thecontroller circuitry and configured to display at least one of anelectrophysiology map or electrical signal indicative of one or moreelectrical characteristics of the contacted tissue, wherein the one ormore electrical signals are independent of the orientation of the planararray catheter relative to the contacted tissue.